- Unknown type - GTR - NCBI

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Unknown type

offered by

GTR Test Accession:

Last updated in GTR:

View version history

GTR000510916.12, last updated: 2019-04-10

GTR000510916.11, last updated: 2019-03-21

GTR000510916.10, last updated: 2017-08-25

GTR000510916.9, last updated: 2016-05-13

GTR000510916.8, last updated: 2015-09-01

GTR000510916.7, last updated: 2014-07-07

GTR000510916.6, last updated: 2014-07-02

GTR000510916.5, last updated: 2014-06-17

GTR000510916.4, last updated: 2014-06-13

GTR000510916.3, last updated: 2014-05-30

GTR000510916.2, last updated: 2014-04-03

GTR000510916.1, registered in GTR: 2014-04-03

At a Glance

Conditions (188):

Angelman syndrome; 2-methyl-3-hydroxybutyric aciduria; ATR-X syndrome more...

Genes (107):

ABCD1 (Xq28); ACSL4 (Xq23); AFF2 (); AGTR2 (Xq23); AIFM1 () more...

Conditions

Total conditions: 188

Condition/Phenotype	Identifier

Methodology

Total methods: 0

Method Category

Test method

Instrument *

* Instrument: Not provided

Technical Information

Recommended fields not provided:

Test Confirmation

Additional Information

Reviews:

PubMed Clinical Queries

Reviews in PubMed

Clinical resources:

Clinicaltrials.gov

Molecular resources:

View SNRPN variations in ClinVar

View UBE3A variations in ClinVar

Coriell Institute for Medical Research

Practice guidelines:

Eurogentest, 2008

Consumer resources:

Genetic Alliance

MedlinePlusGenetics (GHR)

NCATS Office of Rare Diseases Research (GARD)

IMPORTANT NOTE: NIH does not independently verify information submitted to GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.